西亚试剂：Listeria monocytogenes impairs SUMOylation for efficient in

发布时间：2026-01-27

Listeria monocytogenes impairs SUMOylation for efficient infection
David Ribet1,2,3, Mélanie Hamon1,2,3, Edith Gouin1,2,3, Marie-Anne Nahori1,2,3, Francis Impens4,5, Hélène Neyret-Kahn6,7, Kris Gevaert4,5, Jo?l Vandekerckhove4,5, Anne Dejean6,7 & Pascale Cossart1,2,3

Institut Pasteur, Unité des Interactions Bactéries-Cellules, Département de Biologie Cellulaire et Infection, F-75015 Paris, France
INSERM, U604, F-75015 Paris, France
INRA, USC2020, F-75015 Paris, France
Department of Medical Protein Research, VIB, B-9000 Ghent, Belgium
Department of Biochemistry, Ghent University, B-9000 Ghent, Belgium
Institut Pasteur, Unité Organisation Nucléaire et Oncogenèse, Département de Biologie Cellulaire et Infection, F-75015 Paris, France
INSERM, U579, F-75015 Paris, France

During infection, pathogenic bacteria manipulate the host cell in various ways to allow their own replication, propagation and escape from host immune responses. Post-translational modifications are unique mechanisms that allow cells to rapidly, locally and specifically modify activity or interactions of key proteins. Some of these modifications, including phosphorylation and ubiquitylation1, 2, can be induced by pathogens. However, the effects of pathogenic bacteria on SUMOylation, an essential post-translational modification in eukaryotic cells3, remain largely unknown. Here we show that infection with Listeria monocytogenes leads to a decrease in the levels of cellular SUMO-conjugated proteins. This event is triggered by the bacterial virulence factor listeriolysin O (LLO), which induces a proteasome-independent degradation of Ubc9, an essential enzyme of the SUMOylation machinery, and a proteasome-dependent degradation of some SUMOylated proteins. The effect of LLO on Ubc9 is dependent on the pore-forming capacity of the toxin and is shared by other bacterial pore-forming toxins like perfringolysin O (PFO) and pneumolysin (PLY). Ubc9 degradation was also observed in vivo in infected mice. Furthermore, we show that SUMO overexpression impairs bacterial infection. Together, our results reveal that Listeria, and probably other pathogens, dampen the host response by decreasing the SUMOylation level of proteins critical for infection.

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